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rs397508066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common/normal
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar
Make rs397508066(-;AA)
Make rs397508066(AA;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332472
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508066
dbSNP (old)rs397508066
ClinGenrs397508066
ebirs397508066
HLIrs397508066
Exacrs397508066
Gnomadrs397508066
Varsomers397508066
Maprs397508066
PheGenIrs397508066
Biobankrs397508066
1000 genomesrs397508066
hgdprs397508066
ensemblrs397508066
gopubmedrs397508066
geneviewrs397508066
scholarrs397508066
googlers397508066
pharmgkbrs397508066
gwascentralrs397508066
openSNPrs397508066
23andMers397508066
23andMe allrs397508066
SNP Nexus

SNPshotrs397508066
SNPdbers397508066
MSV3drs397508066
GWAS Ctlgrs397508066
Max Magnitude6
ClinVar
Risk rs397508066(A;A) rs397508066(AA;AA)
Alt rs397508066(A;A) rs397508066(AA;AA)
Reference Rs397508066(-;-)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32906608_32906609dupAA; NC_000013.10:g.32906609dupA
CLNSRC ClinVar
CLNACC RCV000045922.2, RCV000045924.2, RCV000241048.2,